Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0003756
Disease: Arenaviridae Infections
Arenaviridae Infections 		1 0 1 0.25 0 0
CUI: C0029163
Disease: Oral Hemorrhage
Oral Hemorrhage 		1 0 1 0.25 0 0
CUI: C0239984
Disease: Increased IgA level
Increased IgA level 		1 1 1 0.25 1 1.00
CUI: C1833172
Disease: Abnormal delayed hypersensitivity skin test
Abnormal delayed hypersensitivity skin test 		1 0 1 0.25 0 0
CUI: C1833173
Disease: Absent microvilli on the surface of peripheral blood lymphocytes
Absent microvilli on the surface of peripheral blood lymphocytes 		1 0 1 0.25 0 0
CUI: C1839164
Disease: Thrombocytopenia, X-Linked, Intermittent
Thrombocytopenia, X-Linked, Intermittent 		1 0 1 0.25 0 0
CUI: C1847711
Disease: NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO
NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO 		1 0 1 0.25 0 0
CUI: C1858977
Disease: Increased IgG level
Increased IgG level 		1 1 1 0.25 1 1.00
CUI: C1866029
Disease: Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma 		1 0 1 0.25 0 0
CUI: C1866031
Disease: Linear arrays of macular hyperkeratoses in flexural areas
Linear arrays of macular hyperkeratoses in flexural areas 		1 0 1 0.25 0 0
CUI: C3711388
Disease: African Hemochromatosis
African Hemochromatosis 		1 0 1 0.25 0 0
CUI: C3840212
Disease: Cannabis withdrawal
Cannabis withdrawal 		1 0 1 0.25 0 0
CUI: C4016481
Disease: WISKOTT-ALDRICH SYNDROME, ATTENUATED
WISKOTT-ALDRICH SYNDROME, ATTENUATED 		1 0 1 0.25 0 0
CUI: C4021766
Disease: Reduced lymphocyte surface expression of CD43
Reduced lymphocyte surface expression of CD43 		1 0 1 0.25 0 0
CUI: C4072911
Disease: Decreased proportion of naive B cells
Decreased proportion of naive B cells 		1 1 1 0.25 1 1.00
CUI: C4072914
Disease: Increased proportion of memory B cells
Increased proportion of memory B cells 		1 1 1 0.25 1 1.00
CUI: C4225219
Disease: IMMUNODEFICIENCY 46
IMMUNODEFICIENCY 46 		1 0 1 0.25 0 0
CUI: C4721383
Disease: Abnormal esophagus morphology
Abnormal esophagus morphology 		1 1 1 0.25 1 1.00
CUI: C4747989
Disease: PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2
PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2 		1 3 1 0.25 1 0.33
CUI: C0392170
Disease: Fibrotic lymphadenopathy
Fibrotic lymphadenopathy 		2 0 1 0.20 0 0
CUI: C0427544
Disease: Monocytopenia
Monocytopenia 		2 0 1 0.20 0 0
CUI: C1839972
Disease: Increased IgM level
Increased IgM level 		2 2 1 0.20 1 0.50
CUI: C3277076
Disease: BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT 		2 0 1 0.20 0 0
CUI: C3278148
Disease: BERNARD-SOULIER SYNDROME, TYPE A1
BERNARD-SOULIER SYNDROME, TYPE A1 		2 0 1 0.20 0 0
CUI: C4021098
Disease: Abnormal natural killer cell morphology
Abnormal natural killer cell morphology 		2 1 1 0.20 1 1.00